Actively Recruiting
Subendocardial Viability Ratio in Hypertension
Led by Istituto Auxologico Italiano · Updated on 2025-08-03
3000
Participants Needed
5
Research Sites
221 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The aim of the research is to evaluate the Subendocardial Viability Ratio (SEVR) in hypertensive patients, using non-invasive arterial tonometry, and to establish the influencing factors and the possibility of predicting cardiovascular morbidity and mortality in arterial hypertension. The SEVR will be evaluated on all patients belonging to the Arterial Hypertension Centers undergoing non-invasive arterial tonometry. The SEVR is calculated on the morphology of the central pressure wave as the ratio between the DPTI (diastolic pressure-time index), i.e. the area between the carotid pressure curve and the ventricular pressure curve during the diastolic phase, and the SPTI ( systolic pressure-time index), i.e. the area under the carotid pressure curve during the systolic phase. The SEVR will be correlated with the anthropometric and pathology variables which will be collected in an appropriate database.
CONDITIONS
Official Title
Subendocardial Viability Ratio in Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hypertension
You will not qualify if you...
- Atrial fibrillation
AI-Screening
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Trial Site Locations
Total: 5 locations
1
Centro di Prevenzione e Cura dell'Ipertensione Arteriosa "Alessandro Filippi"
Mascalucia, Catania, Italy
Actively Recruiting
2
Unità Operativa Semplice Dipartimentale Ipertensione Arteriosa "Anna Maria Pirrelli", Università degli Studi di Bari "Aldo Moro". Policlinico Consorziale di Bari
Bari, Italy
Actively Recruiting
3
Istituto Auxologico Italiano IRCCS
Milan, Italy, 20145
Actively Recruiting
4
Medicina II Cardiovascolare, AUSL-IRCCS di Reggio Emilia
Reggio Emilia, Italy
Actively Recruiting
5
Dipartimento di Scienze Mediche, Chirurgiche e della Salute, Università degli studi di Trieste
Trieste, Italy
Actively Recruiting
Research Team
P
Paolo Salvi, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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